Eriksson B M, Rodriguez-Martinez H
Department of Obstetrics and Gynaecology, Faculty of Veterinary Medicine, Centre for Reproductive Biology (CRB), Swedish University of Agricultural Sciences (SLU), Box 7039, SE-750 07, Uppsala, Sweden.
Anim Reprod Sci. 2000 Nov 1;63(3-4):205-20. doi: 10.1016/s0378-4320(00)00171-8.
The effects of different freezing and thawing rates on the post-thaw motility and membrane integrity of boar spermatozoa, processed as split samples in Maxi-straws or flat PET-plastic packages (FlatPack) were studied. A programmable freezing device was used to obtain freezing rates of either 20, 50 or 80 degrees C/min. Thawing of the samples was performed in a bath of circulating water; for 40s at 50 degrees C or 27s at 70 degrees C for Maxi-straws and 23s at 35 degrees C, 13s at 50 degrees C or 8s at 70 degrees C for the FlatPacks. Sperm motility was assessed both visually and with a computer assisted semen analysis (CASA) apparatus, while plasma membrane integrity was assessed using the fluorescent probes Calcein AM and ethidium homodimer-1. Temperature changes during freezing and thawing were monitored in both forms of packaging. Values for motile spermatozoa, sperm velocity and lateral head displacement variables were significantly (p<0.05) higher for samples frozen in FlatPacks than in Maxi-straws, with superior results at higher thawing rates. Freezing at 50 degrees C/min yielded better motility than 20 or 80 degrees C/min, although the effect was rather small. Neither freezing rate nor thawing rate had any effect on membrane integrity (p>0.05). A significant boar effect was seen for several parameters. The most striking difference in temperature courses between containers was a 4-5-fold lowering of the thawing rate, between -20 and 0 degrees C, in the center of the Maxi-straw, compared with the FlatPack. This is apparently due to the insulating effect of the thawed water in the periphery of the Maxi-straw. The improvement in sperm motility seen when using the FlatPack appears to be related to the rapid thawing throughout the sample, which decreases the risk of cell damage due to recrystallization during thawing. Since sperm motility patterns have been reported to be correlated with fertility both in vitro and in vivo it is speculated that the use of the FlatPack might improve the results when using frozen-thawed boar spermatozoa for artificial insemination.
研究了不同冻融速率对猪精子解冻后活力及膜完整性的影响,精子样本分别以大细管或扁平PET塑料包装(FlatPack)进行分割处理。使用可编程冷冻设备获得20、50或80℃/min的冷冻速率。样本在循环水浴中解冻;大细管在50℃解冻40s或在70℃解冻27s,FlatPack在35℃解冻23s、在50℃解冻13s或在70℃解冻8s。通过视觉和计算机辅助精液分析(CASA)仪器评估精子活力,使用荧光探针钙黄绿素AM和乙锭同二聚体-1评估质膜完整性。监测两种包装形式在冻融过程中的温度变化。FlatPack包装冷冻的样本,其活动精子、精子速度和头部横向位移变量的值显著(p<0.05)高于大细管包装的样本,解冻速率较高时效果更佳。以50℃/min冷冻产生的活力优于20或80℃/min,尽管效果相当小。冷冻速率和解冻速率对膜完整性均无影响(p>0.05)。几个参数存在显著的公猪效应。两种容器之间温度变化过程最显著的差异是,在-20至0℃之间,大细管中心的解冻速率比FlatPack降低了4至5倍。这显然是由于大细管周边解冻水的隔热作用。使用FlatPack时精子活力的提高似乎与整个样本的快速解冻有关,这降低了解冻过程中因再结晶导致细胞损伤的风险。由于据报道精子活力模式在体外和体内均与生育力相关,因此推测使用FlatPack在将冻融猪精子用于人工授精时可能会改善结果。